ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol solution

Isopropyl Rubbing Alcohol by

Drug Labeling and Warnings

Isopropyl Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by McKesson Medical-Surgical Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active Ingredient

Isopropyl Alcohol 70%

Purpose

First Aid Antiseptic

Use

First aid to help prevent the risk of infection in minor cuts, scrapes and burns

Warnings

• For external use only
• Flammable
• Keep away from fire or flame, heat, spark, electrical

• Do not use with electrocautery procedures

• Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns

• When using this product
  • do not get into eyes
  • do not apply over large areas of the body
  • do not use longer than 1 week unless directed by a doctor

• Stop use and ask a doctor if condition persists or gets worse

• Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Clean the affected area
• Apply a small amount of this product 1 to 3 times daily
• May be covered with a sterile bandage
• If bandaged, let dry first

Other Information

• Does not contain, nor is intended as a substitute for grain or ethyl alcohol
• Will produce serious gastric disturbances if taken internally

Inactive Ingredient

purified water

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Distributed By McKesson Medical-Surgical Inc.

Richmond, VA 23233

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

NDC: 68599-2302-6

McKESSON

Isopropyl Rubbing Alcohol 70%

USP | FIRST AID ANTISEPTIC

16 FL OZ (1 PT)
(473 mL)

TAMPER EVIDENT CAP FOR YOUR PROTECTION.
IF RING-BAND IS DETACHED FROM CAP OR MISSING
DO NOT USE.

WARNING:
FLAMMABLE

MFR # 23-D0022

Distributed By McKesson Medical-Surgical Inc.
Richmond, VA 23233

Made in USA

PRINCIPAL DISPLAY PANEL

Drug Facts

PRINCIPAL DISPLAY PANEL

Case

INGREDIENTS AND APPEARANCE

ISOPROPYL RUBBING ALCOHOL 
isopropyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68599-2302
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	700 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68599-2302-6	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/09/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/09/2013

Labeler - McKesson Medical-Surgical Inc. (023904428)